KR20240036127A - 첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물 - Google Patents

첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물 Download PDF

Info

Publication number: KR20240036127A
Authority: KR; South Korea
Prior art keywords: thermoplastic polymer; pigment; polymer composition; group; ppm
Prior art date: 2018-12-21

Application number

KR1020247007412A

Other languages

English (en)

Korean (ko)

Inventor

신페이 유

크리스토퍼 코채노위츠

네이선 멜

케이스 켈러

브렌트 존슨

클리포드 바이넘

Original Assignee

밀리켄 앤드 캄파니

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2018-12-21

Filing date

2019-12-19

Publication date

2024-03-19

2019-12-19 Application filed by 밀리켄 앤드 캄파니 filed Critical 밀리켄 앤드 캄파니

2024-03-19 Publication of KR20240036127A publication Critical patent/KR20240036127A/ko

Links

239000000203 mixture Substances 0.000 title claims abstract description 283
229920001169 thermoplastic Polymers 0.000 title claims abstract description 187
239000000654 additive Substances 0.000 title claims abstract description 67
230000000996 additive effect Effects 0.000 title claims abstract description 56
239000008395 clarifying agent Substances 0.000 claims abstract description 92
239000003086 colorant Substances 0.000 claims abstract description 72
238000002156 mixing Methods 0.000 claims abstract description 15
238000004519 manufacturing process Methods 0.000 claims abstract description 6
239000000049 pigment Substances 0.000 claims description 76
238000000034 method Methods 0.000 claims description 47
-1 bisphenol phosphates Chemical class 0.000 claims description 45
229910052739 hydrogen Inorganic materials 0.000 claims description 40
239000001257 hydrogen Substances 0.000 claims description 40
239000006229 carbon black Substances 0.000 claims description 35
150000002431 hydrogen Chemical class 0.000 claims description 31
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 19
239000001057 purple pigment Substances 0.000 claims description 17
125000000217 alkyl group Chemical group 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 15
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
239000001055 blue pigment Substances 0.000 claims description 14
125000003342 alkenyl group Chemical group 0.000 claims description 13
125000003545 alkoxy group Chemical group 0.000 claims description 12
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 12
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
229920005630 polypropylene random copolymer Polymers 0.000 claims description 9
230000001747 exhibiting effect Effects 0.000 claims description 8
229910019142 PO4 Inorganic materials 0.000 claims description 7
125000003118 aryl group Chemical group 0.000 claims description 7
235000021317 phosphate Nutrition 0.000 claims description 7
229930185605 Bisphenol Natural products 0.000 claims description 6
125000002521 alkyl halide group Chemical group 0.000 claims description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
229920005629 polypropylene homopolymer Polymers 0.000 claims description 6
229920000642 polymer Polymers 0.000 description 43
239000004594 Masterbatch (MB) Substances 0.000 description 18
229920005989 resin Polymers 0.000 description 10
239000011347 resin Substances 0.000 description 10
238000005259 measurement Methods 0.000 description 8
150000005846 sugar alcohols Polymers 0.000 description 8
238000002371 ultraviolet--visible spectrum Methods 0.000 description 8
239000004743 Polypropylene Substances 0.000 description 7
238000002835 absorbance Methods 0.000 description 7
238000002347 injection Methods 0.000 description 7
239000007924 injection Substances 0.000 description 7
229920001155 polypropylene Polymers 0.000 description 7
238000010094 polymer processing Methods 0.000 description 6
238000001125 extrusion Methods 0.000 description 5
229920001223 polyethylene glycol Polymers 0.000 description 5
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 4
150000003934 aromatic aldehydes Chemical class 0.000 description 4
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
XXHCQZDUJDEPSX-KNCHESJLSA-L calcium;(1s,2r)-cyclohexane-1,2-dicarboxylate Chemical compound [Ca+2].[O-]C(=O)[C@H]1CCCC[C@H]1C([O-])=O XXHCQZDUJDEPSX-KNCHESJLSA-L 0.000 description 4
239000000975 dye Substances 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
230000003287 optical effect Effects 0.000 description 4
229920005633 polypropylene homopolymer resin Polymers 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000002253 acid Substances 0.000 description 3
238000011161 development Methods 0.000 description 3
238000000465 moulding Methods 0.000 description 3
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 3
229920000098 polyolefin Polymers 0.000 description 3
229920005606 polypropylene copolymer Polymers 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
230000006641 stabilisation Effects 0.000 description 3
238000011105 stabilization Methods 0.000 description 3
PIYNPBVOTLQBTC-UHFFFAOYSA-N 1-[8-propyl-2,6-bis(4-propylphenyl)-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound O1C2C(CCC)OC(C=3C=CC(CCC)=CC=3)OC2C(C(O)CO)OC1C1=CC=C(CCC)C=C1 PIYNPBVOTLQBTC-UHFFFAOYSA-N 0.000 description 2
239000006057 Non-nutritive feed additive Substances 0.000 description 2
JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 2
239000004904 UV filter Substances 0.000 description 2
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
238000000071 blow moulding Methods 0.000 description 2
XXHCQZDUJDEPSX-UHFFFAOYSA-L calcium;cyclohexane-1,2-dicarboxylate Chemical compound [Ca+2].[O-]C(=O)C1CCCCC1C([O-])=O XXHCQZDUJDEPSX-UHFFFAOYSA-L 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000004040 coloring Methods 0.000 description 2
230000006870 function Effects 0.000 description 2
HNMCSUXJLGGQFO-UHFFFAOYSA-N hexaaluminum;hexasodium;tetrathietane;hexasilicate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].S1SSS1.S1SSS1.[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] HNMCSUXJLGGQFO-UHFFFAOYSA-N 0.000 description 2
KHLVKKOJDHCJMG-QDBORUFSSA-L indigo carmine Chemical compound [Na+].[Na+].N/1C2=CC=C(S([O-])(=O)=O)C=C2C(=O)C\1=C1/NC2=CC=C(S(=O)(=O)[O-])C=C2C1=O KHLVKKOJDHCJMG-QDBORUFSSA-L 0.000 description 2
238000001746 injection moulding Methods 0.000 description 2
239000002667 nucleating agent Substances 0.000 description 2
238000004806 packaging method and process Methods 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
239000010452 phosphate Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
239000012748 slip agent Substances 0.000 description 2
239000004416 thermosoftening plastic Substances 0.000 description 2
235000013799 ultramarine blue Nutrition 0.000 description 2
229910052724 xenon Inorganic materials 0.000 description 2
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
GGQHNQQPLWRNHD-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-11-hydroxy-5h-benzo[d][1,3,2]benzodioxaphosphocine 11-oxide Chemical class C1C2=CC(C(C)(C)C)=CC(C(C)(C)C)=C2OP(O)(=O)OC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C GGQHNQQPLWRNHD-UHFFFAOYSA-N 0.000 description 1
IBABXJRXGSAJLQ-UHFFFAOYSA-N 1,4-bis(2,6-diethyl-4-methylanilino)anthracene-9,10-dione Chemical compound CCC1=CC(C)=CC(CC)=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=C(CC)C=C(C)C=C1CC IBABXJRXGSAJLQ-UHFFFAOYSA-N 0.000 description 1
MBZMDDQWCGCTMH-UHFFFAOYSA-N 1-n,1-n,1-n-tris(2-methylcyclohexyl)methanetricarboxamide Chemical compound CC1CCCCC1NC(=O)C(C(=O)NC1C(CCCC1)C)C(=O)NC1C(C)CCCC1 MBZMDDQWCGCTMH-UHFFFAOYSA-N 0.000 description 1
POQJHLBMLVTHAU-UHFFFAOYSA-N 3,4-Dimethylbenzaldehyde Chemical compound CC1=CC=C(C=O)C=C1C POQJHLBMLVTHAU-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004805 Cyclohexane-1,2-dicarboxylic acid Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
HMEKVHWROSNWPD-UHFFFAOYSA-N Erioglaucine A Chemical compound [NH4+].[NH4+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 HMEKVHWROSNWPD-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
229910003023 Mg-Al Inorganic materials 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
125000004036 acetal group Chemical group 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
125000003172 aldehyde group Chemical group 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
HUMNYLRZRPPJDN-KWCOIAHCSA-N benzaldehyde Chemical group O=[11CH]C1=CC=CC=C1 HUMNYLRZRPPJDN-KWCOIAHCSA-N 0.000 description 1
150000003935 benzaldehydes Chemical class 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
235000013361 beverage Nutrition 0.000 description 1
IVVOCRBADNIWDM-UHFFFAOYSA-N bicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1CC2C(C(O)=O)C(C(=O)O)C1C2 IVVOCRBADNIWDM-UHFFFAOYSA-N 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000000038 blue colorant Substances 0.000 description 1
235000012745 brilliant blue FCF Nutrition 0.000 description 1
239000004161 brilliant blue FCF Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
238000005266 casting Methods 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
230000008094 contradictory effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical class OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
FXDGCBFGSXNGQD-UHFFFAOYSA-L disodium;bicyclo[2.2.1]heptane-2,3-dicarboxylate Chemical compound [Na+].[Na+].C1CC2C(C([O-])=O)C(C(=O)[O-])C1C2 FXDGCBFGSXNGQD-UHFFFAOYSA-L 0.000 description 1
239000003814 drug Substances 0.000 description 1
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238000010101 extrusion blow moulding Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
238000010096 film blowing Methods 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000010102 injection blow moulding Methods 0.000 description 1
238000010103 injection stretch blow moulding Methods 0.000 description 1
238000001990 intravenous administration Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
UADIOTAIECKQLQ-UHFFFAOYSA-M lithium;1,3,7,9-tetratert-butyl-11-oxido-5h-benzo[d][1,3,2]benzodioxaphosphocine 11-oxide Chemical compound [Li+].C1C2=CC(C(C)(C)C)=CC(C(C)(C)C)=C2OP([O-])(=O)OC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C UADIOTAIECKQLQ-UHFFFAOYSA-M 0.000 description 1
238000011068 loading method Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
CNRMAYYJMYPPHU-UHFFFAOYSA-N methanetricarboxamide Chemical class NC(=O)C(C(N)=O)C(N)=O CNRMAYYJMYPPHU-UHFFFAOYSA-N 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
KMQIMDNQSNRDBJ-UHFFFAOYSA-N n-(3,5-diformamidophenyl)formamide Chemical class O=CNC1=CC(NC=O)=CC(NC=O)=C1 KMQIMDNQSNRDBJ-UHFFFAOYSA-N 0.000 description 1
CPEULHAPWXMDDV-UHFFFAOYSA-N n-[3,5-bis(2,2-dimethylpropanoylamino)phenyl]-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC(NC(=O)C(C)(C)C)=CC(NC(=O)C(C)(C)C)=C1 CPEULHAPWXMDDV-UHFFFAOYSA-N 0.000 description 1
JGMMIGGLIIRHFV-UHFFFAOYSA-N nonane-1,2,3,4,5,6,7,8,9-nonol Chemical compound OCC(O)C(O)C(O)C(O)C(O)C(O)C(O)CO JGMMIGGLIIRHFV-UHFFFAOYSA-N 0.000 description 1
239000008188 pellet Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920000306 polymethylpentene Polymers 0.000 description 1
239000011116 polymethylpentene Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
238000001175 rotational moulding Methods 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000992 solvent dye Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
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238000012360 testing method Methods 0.000 description 1
238000003856 thermoforming Methods 0.000 description 1
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UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 1
239000000984 vat dye Substances 0.000 description 1
239000000811 xylitol Substances 0.000 description 1
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
229960002675 xylitol Drugs 0.000 description 1
235000010447 xylitol Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/156—Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring
- C08K5/1575—Six-membered rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/12—Polypropene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2423/10—Homopolymers or copolymers of propene
- C08J2423/12—Polypropene

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Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)

KR1020247007412A 2018-12-21 2019-12-19 첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물 KR20240036127A (ko)

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US201862783316P	2018-12-21	2018-12-21
US62/783,316		2018-12-21
KR1020217022927A KR102646123B1 (ko)	2018-12-21	2019-12-19	첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물
PCT/US2019/067529 WO2020132273A1 (en)	2018-12-21	2019-12-19	Additive compositions and thermoplastic polymer compositions comprising the same

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KR1020217022927A KR102646123B1 (ko)	2018-12-21	2019-12-19	첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물

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US (2)	US11834558B2 (ja)
EP (1)	EP3898811A1 (ja)
JP (2)	JP7339340B2 (ja)
KR (2)	KR20240036127A (ja)
CN (3)	CN117534904A (ja)
BR (1)	BR112021006938A2 (ja)
CA (1)	CA3116291A1 (ja)
WO (1)	WO2020132273A1 (ja)

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2019
- 2019-12-19 WO PCT/US2019/067529 patent/WO2020132273A1/en unknown
- 2019-12-19 US US16/721,199 patent/US11834558B2/en active Active
- 2019-12-19 CN CN202311462479.6A patent/CN117534904A/zh active Pending
- 2019-12-19 KR KR1020247007412A patent/KR20240036127A/ko not_active Application Discontinuation
- 2019-12-19 EP EP19842943.3A patent/EP3898811A1/en active Pending
- 2019-12-19 CA CA3116291A patent/CA3116291A1/en active Pending
- 2019-12-19 CN CN202311462334.6A patent/CN117343435A/zh active Pending
- 2019-12-19 JP JP2021530998A patent/JP7339340B2/ja active Active
- 2019-12-19 KR KR1020217022927A patent/KR102646123B1/ko active IP Right Grant
- 2019-12-19 CN CN201980079640.7A patent/CN113166469B/zh active Active
- 2019-12-19 BR BR112021006938-0A patent/BR112021006938A2/pt active Search and Examination
2023
- 2023-08-24 JP JP2023136233A patent/JP2023179424A/ja active Pending
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KR20210105954A (ko)	2021-08-27
US20240110022A1 (en)	2024-04-04
JP2023179424A (ja)	2023-12-19
CA3116291A1 (en)	2020-06-25
CN113166469B (zh)	2023-11-21
JP2022509992A (ja)	2022-01-25
EP3898811A1 (en)	2021-10-27
US20200199308A1 (en)	2020-06-25
KR102646123B1 (ko)	2024-03-08
CN113166469A (zh)	2021-07-23
CN117534904A (zh)	2024-02-09
WO2020132273A1 (en)	2020-06-25
CN117343435A (zh)	2024-01-05
BR112021006938A2 (pt)	2021-07-13
US11834558B2 (en)	2023-12-05
JP7339340B2 (ja)	2023-09-05

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Publication	Publication Date	Title
US10800902B2 (en)	2020-10-13	Additive compositions and thermoplastic compositions comprising the same
BRPI0610208A2 (pt)	2010-06-01	misturas de composições de aditivo de poliofelina e artigos
DE60318309T2 (de)	2008-12-18	Polyarylenetherzusammensetzungen mit verringerter vergilbung und hoher lichtdurchlässigkeit und daraus hergestellte gegenstände
KR102646123B1 (ko)	2024-03-08	첨가제 조성물, 및 이를 포함하는 열가소성 중합체 조성물
RU2819363C2 (ru)	2024-05-17	Композиции добавок и содержащие их термопластичные полимерные композиции
JP2019127518A (ja)	2019-08-01	核剤組成物、これを含有するオレフィン系樹脂組成物およびその成形品
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JPS61278550A (ja)	1986-12-09	ポリプロピレン混合物製容器